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1.
Britvinite, a new mineral species, has been found in manganese ore at the Långban deposit, Bergslagen ore district, Filipstad, Värmland County, Sweden. Calcite, barytocalcite, brucite, cerussite, and hausmannite are associated minerals. Britvinite occurs as pale yellow to colorless transparent plates with a white streak up to 0.2 × 0.5 × 0.5 mm in size, which are flat parallel to {001}; the luster is adamantine. Thin lamellae are flexible, whereas thick ones are brittle; the Mohs hardness is 3. The cleavage is eminent parallel to {001}. The calculated density is 5.51 g/cm3. In the infrared spectrum of the new mineral, the bands of (OH)?, (CO3)2?, and (BO3)3? are recorded, whereas those corresponding to water molecules are absent. Britvinite is optically biaxial and negative, α = 1.896(2), β = 1.903(2), γ = 1.903(2), 2Vmeas = 20(10), Z≈c. Dispersion is strong, r<v. The chemical composition (electron microprobe; H2O determined with the Alimarin method, CO2, with selective sorption) is (wt %) 7.95 MgO, 71.92 PbO, 0.41 Al2O3, 12.77 SiO2, 2.2 H2O, 2.1 CO2, 2.67 B2O3 (calculated on the basis of structural data); total 100.02. The empirical formula calculated on the basis of 59 anions (O + OH) (Z = 1) is as follows: Pb14.75Mg9.03Si9.73Al0.37O30.76(BO3)3.51(CO3)2.18(OH)11.7. The simplified formula (Z = 2) is Pb7 + x Mg4.5(Si5O14)(BO3)2(CO3)(OH,O)7 (x < 0.5). The crystal structure of britvinite has been studied on a single crystal at 173 K; R = 0.0547. The new mineral is triclinic, space group P $ \bar 1 Britvinite, a new mineral species, has been found in manganese ore at the L?ngban deposit, Bergslagen ore district, Filipstad, V?rmland County, Sweden. Calcite, barytocalcite, brucite, cerussite, and hausmannite are associated minerals. Britvinite occurs as pale yellow to colorless transparent plates with a white streak up to 0.2 × 0.5 × 0.5 mm in size, which are flat parallel to {001}; the luster is adamantine. Thin lamellae are flexible, whereas thick ones are brittle; the Mohs hardness is 3. The cleavage is eminent parallel to {001}. The calculated density is 5.51 g/cm3. In the infrared spectrum of the new mineral, the bands of (OH)−, (CO3)2−, and (BO3)3− are recorded, whereas those corresponding to water molecules are absent. Britvinite is optically biaxial and negative, α = 1.896(2), β = 1.903(2), γ = 1.903(2), 2Vmeas = 20(10), Z≈c. Dispersion is strong, r<v. The chemical composition (electron microprobe; H2O determined with the Alimarin method, CO2, with selective sorption) is (wt %) 7.95 MgO, 71.92 PbO, 0.41 Al2O3, 12.77 SiO2, 2.2 H2O, 2.1 CO2, 2.67 B2O3 (calculated on the basis of structural data); total 100.02. The empirical formula calculated on the basis of 59 anions (O + OH) (Z = 1) is as follows: Pb14.75Mg9.03Si9.73Al0.37O30.76(BO3)3.51(CO3)2.18(OH)11.7. The simplified formula (Z = 2) is Pb7 + x Mg4.5(Si5O14)(BO3)2(CO3)(OH,O)7 (x < 0.5). The crystal structure of britvinite has been studied on a single crystal at 173 K; R = 0.0547. The new mineral is triclinic, space group P ; the unit-cell dimensions are a = 9.3409(8), b = 9.3597(7), c = 18.8333(14) ?, α = 80.365(6)°, β = 75.816(6)°, γ = 59.870(5)°, V = 1378.74(19) ?3. The structure consists of alternating TOT stacks (containing octahedral brucite-like and discontinuous tetrahedral (Si5O14)∞∞ layers) and multilayered [Pb7.1(OH)3.6(CO3)(BO3)1.75(SiO4)0.25]∞∞ blocks. The strongest reflections in the X-ray powder diffraction pattern [d, ? (I, %)(hkl)] are 18.1(100)(001), 3.39(30)(12, 14, 015), 3.02(90)(006, 130, 106, 20, 11), 2.698(70)(332, 134, 030, 1), 2.275(30)(008, 420, 424), 1.867(30)(446, 239, 2.1.10, 18), 1.766(40)(151, 31, 10, 453, 542, 512, 42), 1.519(40)(0.0.12). The mineral has been named in honor of Sergei Nikolaevich Britvin (b. 1965), a Russian mineralogist. The type material of britvinite is deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow. The registration number is 3458/1. Original Russian Text ? N.V. Chukanov, O.V. Yakubovich, I.V. Pekov, D.I. Belakovsky, W. Massa, 2007, published in Zapiski Rossiiskogo Mineralogicheskogo Obshchestva, 2007, Pt CXXXVI, No. 6, pp. 18–25. The new mineral britvinite and its name were accepted by the Commission on New Minerals and Mineral Names, Russian Mineralogical Society, June 7, 2006, and approved by the Commission on New Minerals and Mineral Names, International Mineralogical Association, October 17, 2006.  相似文献   

2.
Micas of the composition K(Fe3–x Mg x )AlSi3 O10(OH)2 (x=0.6, 1.2, 1.8, 2.4 and 3.0, corresponding to ann80phl20, ann60phl40, ann40phl60, ann20phl80 and ann0phl100) were synthesized hydrothermally under controlled oxygen fugacity conditions. Lattice parameters a 0 and b 0 show a distinct linear decrease with increasing Mg content. With increasing ferric iron content a deviation from this linear trend is observed especially within iron rich samples. The tetrahedral rotation angle increases smoothly from 0° in annite to 9.1° in phlogopite. Mössbauer spectra show Fe2+ and Fe3+ on the octahedral M1 and M2 sites and partially also Fe3+ on the tetrahedral site. There is a smooth increase of the quadrupole splitting on both the M1 and the M2 site going from annite to phlogopite, probably due to changes in the lattice contribution to the electric field gradient, assuming a positive correlation between quadrupole splitting and distortion. Fe3+ contents, as determined by Mössbauer spectroscopy, versus oxygen fugacity shows that, depending on the composition of the micas, minimum amounts of Fe3+ are present. For ann80phl20 this minimum amount of Fe3+ is about 8% decreasing to about 1–2% Fe3+ for ann20phl80.The molar volume of each solid solution member has been estimated from the determined relations of the molar volume versus % Fe3+ contents, extrapolated back to 0% Fe3+. Plotting these volumes as a function of Xphl shows that negative excess volume occur in the annitephlogopite join, with the maximum deviation from ideality around X phl=0.3. Margules volume parameters have been constrained as: Wv, AnnPhl=0.018±0.016 J/(bar.mol) and Wv, PhlAnn=-0.391±0.025 J(bar.mol) (three site basis).  相似文献   

3.
Ferrovalleriite, ideally 2(Fe,Cu)S · 1.5Fe(OH)2, a layered hydroxide-sulfide of the valleriite group and an analog of valleriite with Fe instead of Mg in the hydroxide block, has been approved by the IMA Commission on New Minerals, Nomenclature and Classification as a valid mineral species. It was found in the Oktyabr’sky Mine, Noril’sk, Krasnoyarsk krai, Siberia, Russia. Ferrovalleriite occurs in cavities of massive sulfide ore mainly consisting of cubanite and mooihoekite. In different cases, it is associated with magnetite, Fe-rich chlorite-like phyllosilicate, ferrotochilinite, hibbingite, or rhodochrosite. Ferrovalleriite forms crystals flattened on [001] (from scaly to tabular; up to 5 mm across and up to 0.3 mm thick), typically split and curved. Occasionally, they are combined into aggregates up to 1.5 × 2 cm. Ferrovalleriite is dark bronze-colored, with a metallic luster and black streak. The Mohs’ hardness is ca. 1; VHN is 35 kg/mm2. Cleavage is perfect parallel to {001}, mica-like. Individuals are flexible and inelastic. D(calc) = 3.72 g/cm3. In reflected light, ferrovalleriite is pleochroic from yellowish to gray; bireflectance is moderate. Anisotropy is strong, with bluish gray to yellowish beige rotation colors. Reflectance values [R 1–R 2 %, (λ, nm)] are: 15.6–16.6 (470), 14.8–20.5 (546), 14.7–22.3 (589), 14.5–24.1 (650). The IR spectrum shows the presence of (OH) groups bonded with Fe cations and the absence of H2O molecules. The chemical composition of the holotype (wt %; electron microprobe, H content is calculated) is as follows: 0.10 Al, 0.03 Mn, 45.31 Fe, 0.07 Ni, 18.29 Cu, 20.37 S, 15.62 O, 0.98 H, total is 100.77. The empirical formula calculated on the basis of 2 S atoms is: Al0.01Fe2.55Cu0.91S2(OH)3.07 = (Fe1.09Cu0.91)Σ2S2 · (Fe 1.34 2+ Fe 0.12 3+ Al0.01)Σ1.47(OH)3.07. The structure of ferrovalleriite is incommensurate (misfit); two sublattices are present: (1) sulfide sublattice, space group $R\bar 3m$ , R3m or R32; the unit-cell dimensions are: a = 3.792(2), c = 34.06(3) Å, V = 424(1) Å3 and (2) hydroxide sublattice, space group $P\bar 3m1$ , P3m1 or P321; the unit-cell dimensions: a = 3.202(3), c = 11.35(2)Å, V = 100.8(3) Å3. Together with this main polytype modification with three-layer (R-cell, Z = 3) sulfide block, the holotype ferrovalleriite contains the modification with one-layer (P-cell, Z = 1) sulfide block (sulfide sublattice with $P\bar 3m1$ , P3m1 or P321, unit cell dimensions: a = 3.789(4), c = 11.35(1) Å, V = 141(5) Å3). The strongest reflections in the X-ray powder pattern (d, Å-I) are: 5.69–100; 3.268–58; 3.163–36; 1.894–34; 1.871–45.  相似文献   

4.
971349 Che;19 Jie(China Universityseienees,Beijing)The MammaljanShowjng ClimatieF盆uetuat应on—ExamPle of the Early Pleistoceneof Ge。FaunaS AS anMam-malian Faunas from Zhoukoudian,Beijing,China(ESI矛,ISSN 1 005一2321,CN 11一3370/P,4(2),1997,p·275一279,1 graph,1 table,10 ref) By analyses of the four local marnmalianfaunas from Zhoukoudian,Beijing,the EarlyPleistoeene elimatie and eeologieal environ-CN 11一1 905/Q1 53,1 graph,1735(2).1997,P.145一mental ehangespaper.One of1 .90M…  相似文献   

5.
采用pH=9.5～13.0的无镁合成海水进行了Mg(OH)2沉积时B的掺入实验,证实了B(OH)3优先掺入Mg(OH)2的硼同位素分馏特征。在所研究的pH范围内,Mg(OH)2沉积的δ11B均高于无镁合成海水的δ11B,它们之间的硼同位素分馏系数α沉积/海水为1.017 7~1.056 9,平均为1.032 9±0.009 32(SD)。硼同位素的这种分馏特征与无机碳酸盐沉积时的硼同位素分馏存在明显差异,表明B掺入Mg(OH)2沉积具有不同的机理。B在Mg(OH)2沉积上的吸附以及B(OH)3与Mg(OH)2的沉积反应同时存在并相互制约是其主要特征,造成了B(OH)3优先掺入的总结果,这并不意味B(OH)3在掺入的分数上占有优势,相反在所研究的pH范围内,Mg(OH)2沉积的B(OH)3/B(OH)-4大都小于1,因此吸附作用决定了Mg(OH)2沉积中B浓度的变化特征。采用这种模型能很好地解释沉积中B浓度、B在沉积和海水间的分配系数Kd以及沉积与海水间的分馏系数α随海水pH的变化特征。石珊瑚中Mg(OH)2的普遍存在和Mg(OH)2中B(OH)3的优先掺入也许会影响珊瑚的硼同位素组成与海水pH的定量对应关系,给δ11B作为古海水pH的代用指标带来一定的不确定性。  相似文献   

6.
《Applied Geochemistry》2002,17(10):1305-1312
The effect of different drying conditions on the stability of NaNd(CO3)·6H2O and NaEu(CO3)·6H2O and the identity of the decomposition product have been investigated. The rate of decomposition and the nature of the altered phases are dependant on the drying conditions used. When the phases are oven dried at 120 °C, the decomposition is immediate and the phase completely alters to Nd2(CO3)3 or Eu2(CO3)3 respectively. Under less severe drying conditions, the Na rare earth carbonate phases alter to Nd2(CO3)3·8H2O and Eu2(CO3)3·8H2O over a period of 24–48 h, but they can be kept indefinitely in a water saturated environment. The implications for using Nd and Eu as actinide analogues are discussed.  相似文献   

7.
Summary Crystals of K2[Co2(SeO3)3]-2H2O and K2[Ni2(SeO3)3]-2H2O were synthesized under low-hydrothermal conditions. Their structures were determined using single crystal X-ray data up to sin / = 0.7Å-1. [Space group P63/m; a = 9.091(3),9.016(2)Å; c = 7.562(2), 7.476(2)Å; Z = 2; RW = 1.6, 2.5%]. The investigations confirmed that K2[Co2(SeO3)3].2H2O and K2[Ni2(SeO3)3]-2H2O represent the first selenites belonging to the zemannite structure type, a framework structure with wide channels running parallel [0001]. In both compounds four maxima were clearly located in the channel by Fourier summations and attributed to two K atoms and two H2O molecules, each with an occupancy factor of 1/6; a possible ordering scheme (full occupancy) with local symmetry 1 and [6]-coordinated K atoms could be derived for the channel atoms.Zusammenfassung Kristalle von K2[Co2(SeO3)3]-2H2O und K2[Ni2(SeO3)3]-2H2O wurden unter niedrig-hydrothermalen Bedingungen synthetisiert. Die Strukturen wurden unter Verwendung von Einkristallröntgendaten bis sin /= 0.7Å-1 bestimmt. [Raumgruppe P63/m; a = 9.091(3), 9.016(2)Å; c = 7.562(2), 7.476(2)Å; Z = 2; RW = 1.6, 2.5%] Die Untersuchungen bestätigten, daß K2[Co2(SeO3)3] - 2H2O und K2 [Ni2(SeO3)3] - 2H2O als erste Selenite dem Strukturtyp des Zemannits angehören, einer Gerüststruktur mit weiten, parallel [0001] verlaufenden Kanälen. In beiden Verbindungen wurden im Kanal vier Maxima durch Fourier-Summationen eindeutig lokalisiert und zwei Kalium-atomen sowie zwei H2O Molekülen, jeweils mit einem Besetzungsfaktor von 1/6, zugeschrieben. Für die Kanalatome konnte ein möglicher Ordnungszustand (volle Besetzung) mit lokaler Symmetrie 1 und [6]-koordinierten Kaliumatomen abgeleitet werden.
Selenite des Zemannittyps: Kristallstrukturen von K2[Co2(SeO3)3] - 2H2O und K2[Ni2(SeO3)3]-2H2O

Dedicated to Prof. Dr. Josef Zemann at the occasion of his 70th birthday

With 2 Figures  相似文献   

8.
Galgenbergite-(Ce) from the type locality, the railroad tunnel Galgenberg between Leoben and St. Michael, Styria, Austria, was investigated. There it occurs in small fissures of an albite-chlorite schist as very thin tabular crystals building rosette-shaped aggregates associated with siderite, ancylite-(Ce), pyrite and calcite. Electron microprobe analyses gave CaO 9.49, Ce2O3 28.95, La2O3 11.70, Nd2O3 11.86, Pr2O3 3.48, CO2 30.00, H2O 3.07, total 98.55 wt.%. CO2 and H2O calculated by stoichiometry. The empirical formula (based on Ca + REE ∑3.0) is $ \mathrm{C}{{\mathrm{a}}_{1.00 }}{{\left( {\mathrm{C}{{\mathrm{e}}_{1.04 }}\mathrm{L}{{\mathrm{a}}_{0.42 }}\mathrm{N}{{\mathrm{d}}_{0.42 }}\mathrm{P}{{\mathrm{r}}_{0.12 }}} \right)}_{2.00 }}{{\left( {\mathrm{C}{{\mathrm{O}}_3}} \right)}_4}\cdot {{\mathrm{H}}_2}\mathrm{O} $ , and the simplified formula is $ \mathrm{CaC}{{\mathrm{e}}_2}{{\left( {\mathrm{C}{{\mathrm{O}}_3}} \right)}_4}\cdot {{\mathrm{H}}_2}\mathrm{O} $ . According to X-ray single crystal diffraction galgenbergite-(Ce) is triclinic, space group $ P\overline{1},a=6.3916(5) $ , b?=?6.4005(4), c?=?12.3898(9) Å, α?=?100.884(4), β?=?96.525(4), γ?=?100.492(4)°, V?=?483.64(6) Å3, Z?=?2. The eight strongest lines in the powder X-ray diffraction pattern are [d calc in Å/(I)/hkl]: 5.052/(100)/011; 3.011/(70)/0-22; 3.006/(66)/004; 5.899/(59)/-101; 3.900/(51)/1-12; 3.125/(46)/-201; 2.526/(42)/022; 4.694/(38)/-102. The infrared absorption spectrum reveals H2O (OH-stretching mode at 3,489 cm?1, HOH bending mode at 1,607 cm?1) and indicates the presence of distinctly non-equivalent CO3-groups by double and quadruple peaks of their ν1, ν2, ν3 and ν4 modes. The crystal structure of galgenbergite-(Ce) was refined with X-ray single crystal data to R1?=?0.019 for 2,448 unique reflections (I?>?2σ(I)) and 193 parameters. The three cation sites of the structure Ca(1), Ce(2) and Ce(3) have a modest mixed site occupation by Ca and small amount of REE (Ce, La, Pr, Nd) and vice versa. The structure is based on double layers parallel to (001), which are composed of Ca(1)Ce(2)(CO3)2 single layers with an ordered chessboard like arrangement of Ca and Ce, and with a roof tile-like stacking of the CO3 groups. Perpendicular to (001) the double layers are connected to a triclinic framework structure with good cleavage parallel to (001) by a differently organized and more open part of the structure formed by Ce(3)(CO3)2(H2O). Based on the topology of the CaCe(CO3)2 single layer in galgenbergite-(Ce), structural relationships to rutherfordine, to aragonite and ancylite type minerals, and to lanthanite are outlined.  相似文献   

9.
Mineralogy and Petrology - Batagayite, CaZn2(Zn,Cu)6(PO4)4(PO3OH)3·12H2O, is a new secondary phosphate mineral from the Këster deposit, Arga-Ynnykh-Khai massif, NE Yakutia, Russia. It is...  相似文献   

10.
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11.
Natural barbosalite Fe2+Fe3+ 2 (PO4)2(OH)2 from Bull Moose Mine, South Dakota, U.S.A., having ideal composition, was investigated with single crystal X-ray diffraction techniques, Mössbauer spectroscopy and SQUID magnetometry to redetermine crystal structure, valence state of iron and evolution of 57Fe Mössbauer parameter and to propose the magnetic structure at low temperatures. At 298?K the title compound is monoclinic, space group P21/n, a o ?= 7.3294(16)?Å, b o ?=?7.4921(17)?Å, c o ?=?7.4148 (18)?Å, β?=?118.43(3)°, Z?=?2. No crystallographic phase transition was observed between 298?K and 110?K. Slight discontinuities in the temperature dependence of lattice parameters and bond angles in the range between 150?K and 180?K are ascribed to the magnetic phase transition of the title compound. At 298?K the Mössbauer spectrum of the barbosalite shows two paramagnetic components, typical for Fe2+ and Fe3+ in octahedral coordination; the area ratio Fe3+/Fe2+ is exactly two, corresponding to the ideal value. Both the Fe2+ and the Fe3+ sublattice order magnetically below 173?K and exhibit a fully developed magnetic pattern at 160?K. The electric field gradient at the Fe2+ site is distorted from axial symmetry with the direction of the magnetic field nearly perpendicular to Vzz, the main component of the electric field gradient. The temperature dependent magnetic susceptibility exhibits strong antiferromagnetic ordering within the corner-sharing Fe3+-chains parallel to [101], whereas ferromagnetic coupling is assumed within the face-sharing [1?1?0] and [?1?1?0] Fe3+-Fe2+-Fe3+ trimer, connecting the Fe3+-chains to each other.  相似文献   

12.
The water-pressure and temperature stability fields of clinohumite-OH, chondrodite-OH and phase A were determined in reversed equilibrium experiments up to 100 kbar within the system MgO–SiO2–H2O. Their PT-fields differ from results from former synthesis experiments. Bracketing experiments on the reaction phase A + low P-clinoenstatite ⇆ forsterite + water resulted in a slightly steeper dP/dT-slope compared to earlier experiments for this equilibrium. Clinohumite-OH and chondrodite-OH both have large stability fields which extend over pressure ranges of more than 80 kbar. However, they are hardly relevant as hydrous minerals within the subducted oceanic lithosphere. Both are too Mg-rich for a typical mantle bulk composition. In addition, the dehydration of subducted oceanic lithosphere – due to (forsterite + water)-forming reactions – will occur before the two humite-group phases even become stable. Restricted to the cool region of cold subducting slabs, phase A, however, might be formed via the reactions phase A + low P-/high P-clinoenstatite ⇆ forsterite + water or antigorite + brucite ⇆ phase A + water, before dehydration of the oceanic lithosphere occurs. Received: 22 July 1997 / Accepted: 12 March 1998  相似文献   

13.
Summary Niedermayrite, Cu4Cd(SO4)2(OH)6 · 4H2O, is a new mineral discovered in 1995 in the Km3-area of the Lavrion mining district, Greece. It forms tiny euhedral plates, commonly intergrown as green crusts up to several cm2 in size on a matrix consisting of a brecciated marble with sphalerite, chalcopyrite, galena, greenockite, hawleyite and pyrite. Associated secondary minerals are gypsum, malachite, chalcanthite, brochantite, hemimorphite, hydrozincite, aurichalcite, one unknown Cd-sulfate, monteponite and otavite. Niedermayrite is non-fluorescent and has a bluish-green colour with vitreous lustre, the streak is white. The crystals are brittle with perfect cleavage parallel {010}. Optics: biaxial (–) with n(calc.), n, and n =1.609, 1.642(2), and 1.661(2), respectively; orientation n//b. The calculated density is 3.292 gcm–3. The most prominent form is {010}. Analysis by electron microprobe gives CdO 16.5, CuO 45.7, SO3 21.6, H2O 16.2 wt.% (calc. to 100% sum) and the empirical formula Cu4.29Cd0.96S2.01O11.28 · 6.71 H2O (based on 18 oxygens p.f.u.). By TGA an H2O content of 18.9 wt.% was obtained. The ideal formula (confirmed by the crystal structure refinement) is Cu4Cd(SO4)2(OH)6 · 4H2O with a theoretical H2O content of 17.2 wt.%. The strongest lines in the X-ray powder diffraction pattern (Gandolfi camera, visually estimated I, refined lattice parameters a = 5.535(2), b = 21.947(9), c = 6.085(2) Å, = 91.98(3)°) are: (dobs[Å]/Iobs/hkl) (11.02/90/0 2 0), (5.874/20/0 1 1), (5.496/100/0 4 0), (5.322/25/0 2 1), (4.079/50/0 4 1), (3.660/20/0 6 0), (3. 437/30/1 5 0), (3.243/40/1 4 1), (2.470/30/2 4 0), (2.425/20/1 4 –2), (2.205/20/2 6 0) and (1.897/20/1 8 2). The mineral is monoclinic, P21/m, Z = 2, a = 5.543(1) Å, b = 21.995(4) Å, c = 6.079(1) Å, = 92.04(3)°, V = 740.7(2) Å3. The crystal structure was determined by single crystal X-ray methods and was refined to R1= 0.026, wR2 = 0.056. The structure of niedermayrite is characterized by 2 [Cu4(OH)6O2]2– sheets of edgesharing Cu coordination octahedra parallel to (010) with attached SO4 tetrahedra, and intercalated CdO2(H2O)4 octahedra with a system of hydrogen bonds. Close relationships to the crystal structures of christelite and campigliaite exist. The new mineral is named for Dr. Gerhard Niedermayr, Naturhistorisches Museum Wien, Austria.
Niedermayrit, Cu4Cd(SO4)2(OH)6 · 4H2O, ein neues Mineral aus dem Bergbaugebiet Lavrion, Griechenland
Zusammenfassung Niedermayrit, Cu4Cd(SO4)2(OH)6 · 4H2O, ist ein neues Mineral, das 1995 im Km3-Bereich des Bergbaugebietes Lavrion, Griechenland, gefunden wurde. Es bildet winzige gut ausgebildete Plättchen, häufig miteinander verwachsen in grünen Krusten bis zu mehreren cm2 Größe. Die Matrix besteht aus brecciösem Marmor mit Sphalerit, Chalcopyrit, Galenit, Greenockit, Hawleyit und Pyrit. Sekundäre Begleitminerale sind Gips, Malachit, Chalcanthit, Brochantit, Hemimorphit, Hydrozincit, Aurichalcit, ein unbekanntes Cd-Sulfat, Monteponit und Otavit. Niedermayrit fluoresziert nicht, besitzt blaugrüne Farbe mit Glasglanz, der Strich ist weiß. Die Kristalle sind spröd mit perfekter Spaltbarkeit parallel {010}. Optik: biaxial (–) mit n(ber.), n, und n=1.609, 1.642(2), und 1.661(2); Orientierung n//b. Die berechnete Dichte beträgt 3.292 gcm–3. Die auffallendste Flächenform ist {010}. Die chemische Analyse mittels Mikrosonde ergibt CdO 16.5, CuO 45.7, SO3 21.6, H2O 16.2wt.% (ber. auf 100% Summe) und die empirische Formel Cu4.29Cd0.96S2.01O11.28 · 6.71 H2O (basierend auf 18 Sauerstoffatomen pro Formeleinheit). Aus der TGA wurde ein H2O Gehalt von 18.9 Gew.% erhalten. Die Idealformel (bestätigt durch die Kristallstrukturverfeinerung) ist Cu4Cd(SO4)2(OH)6 · 4H2O bei einem theoretischen H2O-Gehalt von 17.2 Gew.%. Die stärksten Linien im Pulverdiffraktogramm (Gandolfi Kamera, visuell geschätzte I, verfeinerte Gitterkonstanten a = 5.535(2), b = 21.947(9), c = 6.085(2) Å, = 91.98(3)°) sind: (dobs[Å]/Iobs/hkl) (11.02/90/0 2 0), (5.874/20/0 1 1), (5.496/100/0 4 0), (5.322/25/0 2 1), (4.079/50/0 4 1), (3.660/20/0 6 0), (3.437/30/1 5 0), (3.243/40/1 4 1), (2.470/30/2 4 0), (2.425/20/1 4 –2), (2.205/20/2 6 0) und (1.897/20/1 8 2). Das Mineral ist monoklin, P21/m, Z = 2, a = 5.543(1) Å, b = 21.995(4) Å, c = 6.079(1) Å, = 92.04(3)°, V = 740.7(2) Å3 Die Kristallstruktur wurde mittels Einkristallröntgenmethoden bestimmt und zu R1 = 0.026, wR2 = 0.056 verfeinert. Die Struktur von Niedermayrit ist durch 2 [Cu4(OH)6O2]2– Schichten von kantenverknüpften Cu-Koordinationsoktaedern parallel (010) gekennzeichnet mit damit verbundenen SO4 Tetraedern und dazwischen befindlichen CdO2(H2O)4 Oktaedem mit einem Wasserstoffbrückensystem. Es bestehen enge Beziehungen mit den Kristallstrukturen von Christelit und Campigliait. Das neue Mineral ist nach Dr. Gerhard Niedermayr, Naturhistorisches Museum Wien, Österreich, benannt.

With 7 Figures  相似文献   

14.
采用密度泛函方法计算了水溶液中B(OH)3和B(OH)4-间硼同位素的平衡分馏参数。在模拟液相环境时,采用基于分子簇模型的"水滴"法,分别以6、12、18、24和30个水分子环绕兴趣分子的方式构建"水滴"。对纯水体系的计算结果显示该分馏参数在25?C时为1.031,与实验测定值吻合地非常理想。对不同个数水分子所形成的液相构型进行比较,发现在计算硼同位素的分馏时,12个水分子的"水滴"构型是比较经济和准确的建模方式。此外,我们还讨论了前人对该体系分馏计算中存在的不足,并提出了将分子簇模型扩展到碳酸盐矿物形成过程中硼同位素分馏研究的可能。  相似文献   

15.
《Geochimica et cosmochimica acta》1999,63(13-14):1969-1980
The solubility of ettringite (Ca6[Al(OH)6]2(SO4)3 · 26H2O) was measured in a series of dissolution and precipitation experiments at 5–75°C and at pH between 10.5 and 13.0 using synthesized material. Equilibrium was established within 4 to 6 days, with samples collected between 10 and 36 days. The log KSP for the reaction Ca6[Al(OH)6]2(SO4)3 · 26H2O ⇌ 6Ca2+ + 2Al(OH)4− + 3SO42− + 4OH− + 26H2O at 25°C calculated for dissolution experiments (−45.0 ± 0.2) is not significantly different from the log KSP calculated for precipitation experiments (−44.8 ± 0.4) at the 95% confidence level. There is no apparent trend in log KSP with pH and the mean log KSP,298 is −44.9 ± 0.3. The solubility product decreased linearly with the inverse of temperature indicating a constant enthalpy of reaction from 5 to 75°C. The enthalpy and entropy of reaction ΔH°r and ΔS°r, were determined from the linear regression to be 204.6 ± 0.6 kJ mol−1 and 170 ± 38 J mol−1 K−1. Using our values for log KSP, ΔH°r, and ΔS°r and published partial molal quantities for the constituent ions, we calculated the free energy of formation ΔG°f,298, the enthalpy of formation ΔH°f,298, and the entropy of formation ΔS°f,298 to be −15211 ± 20, −17550 ± 16 kJ mol−1, and 1867 ± 59 J mol−1 K−1. Assuming ΔCP,r is zero, the heat capacity of ettringite is 590 ± 140 J mol−1 K−1.  相似文献   

16.
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17.
A new mineral kobyashevite, Cu5(SO4)2(OH)6·4H2O (IMA 2011–066), was found at the Kapital’naya mine, Vishnevye Mountains, South Urals, Russia. It is a supergene mineral that occurs in cavities of a calcite-quartz vein with pyrite and chalcopyrite. Kobyashevite forms elongated crystals up to 0.2 mm typically curved or split and combined into thin crusts up to 1?×?2 mm. Kobyashevite is bluish-green to turquoise-coloured. Lustre is vitreous. Mohs hardness is 2½. Cleavage is {010} distinct. D(calc.) is 3.16 g/cm3. Kobyashevite is optically biaxial (?), α 1.602(4), β 1.666(5), γ 1.679(5), 2 V(meas.) 50(10)°. The chemical composition (wt%, electron-microprobe data) is: CuO 57.72, ZnO 0.09, FeO 0.28, SO3 23.52, H2O(calc.) 18.39, total 100.00. The empirical formula, calculated based on 18 O, is: Cu4.96Fe0.03Zn0.01S2.01O8.04(OH)5.96·4H2O. Kobyashevite is triclinic, $ P\overline{\,1 } $ , a 6.0731(6), b 11.0597(13), c 5.5094(6)?Å, α 102.883(9)°, β 92.348(8)°, γ 92.597(9)°, V 359.87(7)?Å3, Z?=?1. Strong reflections of the X-ray powder pattern [d,Å-I(hkl)] are: 10.84–100(010); 5.399–40(020); 5.178–12(110); 3.590–16(030); 2.691–16(20–1, 040, 002), 2.653–12(04–1, 02–2), 2.583–12(2–11, 201, 2–1–1), 2.425–12(03–2, 211, 131). The crystal structure (single-crystal X-ray data, R?=?0.0399) сontains [Cu4(SO4)2(OH)6] corrugated layers linked via isolated [CuO2(H2O)4] octahedra; the structural formula is CuCu4(SO4)2(OH)6·4H2O. Kobyashevite is a devilline-group member. It is named in memory of the Russian mineralogist Yuriy Stepanovich Kobyashev (1935–2009), a specialist on mineralogy of the Urals.  相似文献   

18.
This is the first detailed account of the copper sulfate posnjakite (Cu4(SO4)(OH)6·H2O) coating cm-long filaments of a microbial consortium of four cyanobacteria and Herminiimonas arsenicoxydans. It was first observed on immersed plant leaves and stalks in a quarry sump of the abandoned Yanqul gold mine in the northern region of Oman; rock surfaces in the immediate vicinity show no immediate evidence of posnjakite. However, a thin unstructured layer without filaments but also containing the brightly coloured turquoise posnjakite covers ferruginous muds in the sump. Although copper is a potent bactericide, the microbes seem to survive even at the extreme heavy metal concentrations that commonly develop in the sump during the dry season (Cu2+ ≈ 2300 ppm; Zn2+ = 750 ppm; Fe2+ ≈ 120 ppm; Ni2+ = 37 ppm; Crtotal = 2.5 ppm; Cl− = 8250 ppm; and SO42− = 12,250 ppm; pH ∼2.6), thus leading to the precipitation of posnjakite over a large range of physicochemical conditions. Upon exposure to the prevailing arid climate, dehydration and carbonation quickly replace posnjakite with brochantite (Cu4(SO4)(OH)6) and malachite (Cu2(CO3)(OH)2). To characterise and understand the geochemical conditions in which posnjakite precipitates from undersaturated fluids (according to our thermodynamic modelling of the dominant elements), waters from rainy and dry periods were analysed together with various precipitates and compared with the observed field occurrences. The findings imply that posnjakite should not form in the examined environment through purely inorganic mechanisms and its origin must, therefore, be linked to the encountered microbial activities.  相似文献   

19.
该种方法利用离子色谱仪的电导检测器与电化学检测器串联 ,十几分钟即可连续完成水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3 的测定 ,方法具有快速、高效、方便、灵敏、选择性好等特点。方法的检出限分别为 :S2 - 12 5 μg/L ;SO2 - 3 2 2 4 μg/L ;SO2 - 45 0 μg/L ;S2 O2 - 35 0 μg/L。相对标准偏差在 1 5 %～ 6 9%之间 ,能够满足水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3四种阴离子分析测试的需要。  相似文献   

20.
Albrechtschraufite, MgCa4F2[UO2(CO3)3]2?17-18H2O, triclinic, space group Pī, a?=?13.569(2), b?=?13.419(2), c?=?11.622(2) Å, α?=?115.82(1), β?=?107.61(1), γ?=?92.84(1)° (structural unit cell, not reduced), V?=?1774.6(5) Å3, Z?=?2, D c?=?2.69 g/cm3 (for 17.5 H2O), is a mineral that was found in small amounts with schröckingerite, NaCa3F[UO2(CO3)3](SO4)?10H2O, on a museum specimen of uranium ore from Joachimsthal (Jáchymov), Czech Republic. The mineral forms small grain-like subhedral crystals (≤ 0.2 mm) that resemble in appearance liebigite, Ca2[UO2(CO3)3]??~?11H2O. Colour pale yellow-green, luster vitreous, transparent, pale bluish green fluorescence under ultraviolet light. Optical data: Biaxial negative, nX?=?1.511(2), nY?=?1.550(2), nZ?=?1.566(2), 2?V?=?65(1)° (λ?=?589 nm), r < v weak. After qualitative tests had shown the presence of Ca, U, Mg, CO2 and H2O, the chemical formula was determined by a crystal structure analysis based on X-ray four-circle diffractometer data. The structure was later on refined with data from a CCD diffractometer to R1?=?0.0206 and wR2?=?0.0429 for 9,236 independent observed reflections. The crystal structure contains two independent [UO2(CO3)3]4? anions of which one is bonded to two Mg and six Ca while the second is bonded to only one Mg and three Ca. Magnesium forms a MgF2(Ocarbonate)3(H2O) octahedron that is linked via the F atoms with three Ca atoms so as to provide each F atom with a flat pyramidal coordination by one Mg and two Ca. Calcium is 7- and 8-coordinate forming CaFO6, CaF2O2(H2O)4, CaFO3(H2O)4 and CaO2(H2O)6 coordination polyhedra. The crystal structure is built up from MgCa3F2[UO2(CO3)3]?8H2O layers parallel to (001) which are linked by Ca[UO2(CO3)3]?5H2O moieties into a framework of the composition MgCa4F2[UO2(CO3)3]?13H2O. Five additional water molecules are located in voids of the framework and show large displacement parameters. One of the water positions is partly vacant, leading to a total water content of 17-18H2O per formula unit. The MgCa3F2[UO2(CO3)3]?8H2O layers are pseudosymmetric according to plane group symmetry cmm. The remaining constituents do not sustain this pseudosymmetry and make the entire structure truly triclinic. A characteristic paddle-wheel motif Ca[UO2(CO3)3]4Ca relates the structure of albrechtschraufite partly to that of andersonite and two synthetic alkali calcium uranyl tricarbonates.  相似文献   

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